Bennett A B, O'neill S D, Spanswick R M
Section of Plant Biology, Division of Biological Sciences, Cornell University, Ithaca, New York 14853.
Plant Physiol. 1984 Mar;74(3):538-44. doi: 10.1104/pp.74.3.538.
Microsomal membranes isolated from red beet (Beta vulgaris L.) storage tissue were found to contain high levels of ionophore-stimulated ATPase activity. The distribution of this ATPase activity on a continuous sucrose gradient showed a low density peak (1.09 grams per cubic centimeter) that was stimulated over 400% by gramicidin and coincided with a peak of NO(3) (-)-sensitive ATPase activity. At higher densities (1.16-1.18 grams per cubic centimeter) a shoulder of gramicidin-stimulated ATPase that coincided with a peak of vanadate-sensitive ATPase was apparent. A discontinuous sucrose gradient of 16/26/34/40% sucrose (w/w) was effective in routinely separating the NO(3) (-)-sensitive ATPase (16/26% interface) from the vanadate-sensitive ATPase (34/40% interface). Both membrane fractions were shown to catalyze ATP-dependent H(+) transport, with the transport process showing the same differential sensitivity to NO(3) (-) and vanadate as the ATPase activity.Characterization of the lower density ATPase (16/26% interface) indicated that it was highly stimulated by gramicidin, inhibited by KNO(3), stimulated by anions (Cl(-) > Br(-) > acetate > HCO(3) (-) > SO(4) (2-)), and largely insensitive to monovalent cations. These characteristics are very similar to those reported for tonoplast ATPase activity and a tonoplast origin for the low density membrane vesicles was supported by comparison with isolated red beet vacuoles. The membranes isolated from the vacuole preparation were found to possess an ATPase with characteristics identical to those of the low density membrane vesicles, and were shown to have a peak density of 1.09 grams per cubic centimeter. Furthermore, following osmotic lysis the vacuolar membranes apparently resealed and ATP-dependent H(+) transport could be demonstrated in these vacuole-derived membrane vesicles. This report, thus, strongly supports a tonoplast origin for the low density, anion-sensitive H(+)-ATPase and further indicates the presence of a higher density, vanadate-sensitive, H(+)-ATPase in the red beet microsomal membrane fraction, which is presumably of plasma membrane origin.
从红甜菜(Beta vulgaris L.)贮藏组织中分离出的微粒体膜被发现含有高水平的离子载体刺激的ATP酶活性。这种ATP酶活性在连续蔗糖梯度上的分布显示出一个低密度峰(每立方厘米1.09克),短杆菌肽可使其刺激超过400%,且与对NO(3) (-)敏感的ATP酶活性峰重合。在更高密度(每立方厘米1.16 - 1.18克)时,短杆菌肽刺激的ATP酶出现一个肩峰,与对钒酸盐敏感的ATP酶峰重合。16/26/34/40%(重量/重量)的不连续蔗糖梯度能有效地常规分离出对NO(3) (-)敏感的ATP酶(16/26%界面处)和对钒酸盐敏感的ATP酶(34/40%界面处)。两个膜组分均显示能催化ATP依赖的H(+)转运,转运过程对NO(3) (-)和钒酸盐的敏感性与ATP酶活性相同。对低密度ATP酶(16/26%界面处)的特性表征表明,它受短杆菌肽高度刺激,受KNO(3)抑制,受阴离子刺激(Cl(-) > Br(-) > 醋酸盐 > HCO(3) (-) > SO(4) (2-)),且对单价阳离子基本不敏感。这些特性与液泡膜ATP酶活性报道的特性非常相似,通过与分离出的红甜菜液泡比较,支持了低密度膜泡起源于液泡膜的观点。从液泡制备物中分离出的膜被发现具有一种ATP酶,其特性与低密度膜泡的ATP酶相同,且显示出每立方厘米1.09克的峰密度。此外,渗透裂解后,液泡膜明显重新封闭,且在这些源自液泡的膜泡中可证明存在ATP依赖的H(+)转运。因此,本报告有力地支持了低密度、对阴离子敏感的H(+)-ATP酶起源于液泡膜的观点,并进一步表明红甜菜微粒体膜组分中存在一种更高密度、对钒酸盐敏感的H(+)-ATP酶,推测其起源于质膜。